O-mannosyl glycans: from yeast to novel associations with human disease

被引:116
作者
Willer, T [1 ]
Valero, MC
Tanner, W
Cruces, J
Strahl, S
机构
[1] Univ Regensburg, Lehrstuhl Zellbiol & Pflanzenphysiol, D-93040 Regensburg, Germany
[2] Inst Invest Biomed, Dept Bioquim, Madrid, Spain
[3] Univ Autonoma Madrid, Fac Med, CSIC, E-28029 Madrid, Spain
关键词
D O I
10.1016/j.sbi.2003.09.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In yeasts and other fungi, O-mannosyl glycans constitute a major protein modification that is essential for cell viability. For several decades, protein O-mannosylation was considered a yeast-specific modification. Thus, it was especially interesting when it became evident that O-mannosyl glycans in mammals are not as rare as previously thought. O-mannosyl glycans are abundant in the mammalian brain and are also an abundant modification of of alpha-dystroglycan, a component of the dystrophin-glycoprotein complex. Recently, mutations in genes that are or might be involved in the glycosylation of alpha-dystroglycan have been identified. Their association with neuromuscular diseases has focused the attention of different research areas on protein O-mannosylation.
引用
收藏
页码:621 / 630
页数:10
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